Similar articles for PMID: 24142793

Year	Number of Results
2006	6
2007	7
2008	9
2009	10
2010	7
2011	7
2012	11
2013	8
2014	13
2015	11
2016	11
2017	6
2018	3
2019	5
2020	6
2021	5
2022	4
2023	2
2024	0

1

A novel germline JAK2 mutation in familial myeloproliferative neoplasms.

Rumi E, Harutyunyan AS, Casetti I, Pietra D, Nivarthi H, Moriggl R, Cleary C, Bagienski K, Astori C, Bellini M, Berg T, Passamonti F, Kralovics R, Cazzola M. Rumi E, et al. Am J Hematol. 2014 Jan;89(1):117-8. doi: 10.1002/ajh.23614. Am J Hematol. 2014. PMID: 24142793 Free article. No abstract available.

2

The role of the JAK2 GGCC haplotype and the TET2 gene in familial myeloproliferative neoplasms.

Olcaydu D, Rumi E, Harutyunyan A, Passamonti F, Pietra D, Pascutto C, Berg T, Jäger R, Hammond E, Cazzola M, Kralovics R. Olcaydu D, et al. Haematologica. 2011 Mar;96(3):367-74. doi: 10.3324/haematol.2010.034488. Epub 2010 Dec 20. Haematologica. 2011. PMID: 21173100 Free PMC article.

3

Functional analysis of atypical mutations in exons 13 and 15 of JAK2 gene in myeloproliferative neoplasms.

Luo M, Tian T, Zhang Y, Zhang X, Xie J, Xu J, Ren W, Tian C, Wang J, Tan Y, Wang H, Chen X. Luo M, et al. Int J Lab Hematol. 2021 Jun;43(3):e110-e113. doi: 10.1111/ijlh.13398. Epub 2020 Nov 27. Int J Lab Hematol. 2021. PMID: 33244866 No abstract available.

4

Myeloid neoplasm with translocation t(2;11)(p21;q23-24), elevated microRNA 125b-1, and JAK2 exon 12 mutation.

McCormick SR, Higgins RR, Grutkoski PS, Bousquet M, Quelen C, Bartholomaus LM, Brousset P. McCormick SR, et al. Br J Haematol. 2015 Apr;169(2):290-3. doi: 10.1111/bjh.13190. Epub 2014 Oct 15. Br J Haematol. 2015. PMID: 25316507 Free article. No abstract available.

5

[JAK2 mutation and thrombosis - recommendations for screening].

Held M. Held M. Dtsch Med Wochenschr. 2012 Feb;137(5):227. doi: 10.1055/s-0031-1298871. Epub 2012 Jan 25. Dtsch Med Wochenschr. 2012. PMID: 22278696 German. No abstract available.

6

Genetic and clinical implications of the Val617Phe JAK2 mutation in 72 families with myeloproliferative disorders.

Bellanné-Chantelot C, Chaumarel I, Labopin M, Bellanger F, Barbu V, De Toma C, Delhommeau F, Casadevall N, Vainchenker W, Thomas G, Najman A. Bellanné-Chantelot C, et al. Blood. 2006 Jul 1;108(1):346-52. doi: 10.1182/blood-2005-12-4852. Epub 2006 Mar 14. Blood. 2006. PMID: 16537803 Free article.

7

Mutation profile of JAK2 transcripts in patients with chronic myeloproliferative neoplasias.

Ma W, Kantarjian H, Zhang X, Yeh CH, Zhang ZJ, Verstovsek S, Albitar M. Ma W, et al. J Mol Diagn. 2009 Jan;11(1):49-53. doi: 10.2353/jmoldx.2009.080114. Epub 2008 Dec 12. J Mol Diagn. 2009. PMID: 19074595 Free PMC article.

8

Splenomegaly and the JAK2 V617F mutation.

Langabeer SE. Langabeer SE. Eur J Intern Med. 2017 Jan;37:e45-e46. doi: 10.1016/j.ejim.2016.09.026. Epub 2016 Oct 7. Eur J Intern Med. 2017. PMID: 27727073 No abstract available.

9

Germline RBBP6 mutations in familial myeloproliferative neoplasms.

Harutyunyan AS, Giambruno R, Krendl C, Stukalov A, Klampfl T, Berg T, Chen D, Milosevic Feenstra JD, Jäger R, Gisslinger B, Gisslinger H, Rumi E, Passamonti F, Pietra D, Müller AC, Parapatics K, Breitwieser FP, Herrmann R, Colinge J, Bennett KL, Superti-Furga G, Cazzola M, Hammond E, Kralovics R. Harutyunyan AS, et al. Blood. 2016 Jan 21;127(3):362-5. doi: 10.1182/blood-2015-09-668673. Epub 2015 Nov 16. Blood. 2016. PMID: 26574608 Free PMC article. No abstract available.

10

JAK2 (V617F) as an acquired somatic mutation and a secondary genetic event associated with disease progression in familial myeloproliferative disorders.

Rumi E, Passamonti F, Pietra D, Della Porta MG, Arcaini L, Boggi S, Elena C, Boveri E, Pascutto C, Lazzarino M, Cazzola M. Rumi E, et al. Cancer. 2006 Nov 1;107(9):2206-11. doi: 10.1002/cncr.22240. Cancer. 2006. PMID: 16998940 Free article.

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